{"title":"Standardized totally endoscopic non-robotic mitral valve repair for degenerative mitral regurgitation: early single-center outcomes in 84 patients.","authors":"Phan Quang Thuan, Pham Tran Viet Chuong, Cao Dang Khang, Nguyen Hoang Dinh","doi":"10.21542/gcsp.2026.30","DOIUrl":null,"url":null,"abstract":"<p><p><b>Objective:</b> To evaluate early clinical and echocardiographic outcomes of totally endoscopic, non-robotic mitral valve repair for degenerative mitral regurgitation using a standardized DCT approach (double-port; camera and main working port in the same intercostal space; skin incision <3 cm), and to propose operational criteria for \"totally endoscopic\" mitral surgery. <b>Methods:</b> In this single-center observational study, 84 consecutive patients with severe degenerative mitral regurgitation meeting 2021 ESC/EACTS surgical criteria underwent totally endoscopic non-robotic repair with three-dimensional visualization between July 2023 and January 2026. The technique used a primary skin incision ≤3 cm with no rib spreading in all cases. Clinical and echocardiographic outcomes within 30 days were assessed. <b>Results:</b> Repair was successful in all 84 patients (100%), without conversion to sternotomy or replacement. All underwent ring annuloplasty; neochordal implantation was performed in 69 (82.1%). Mean incision length was 2.9 ± 0.3 cm. Mean cardiopulmonary bypass and cross-clamp times were 163.3 ± 50.5 and 112.1 ± 37.5 minutes, respectively. There was no 30-day mortality. Major complications each occurred in 1 patient (1.2%): re-exploration for bleeding, intracranial hemorrhage, and femoral artery occlusion. Median intensive care unit and hospital stays were 2 (IQR 2-3) and 10 (IQR 9-14) days. Echocardiography showed no residual regurgitation ≥ moderate and preserved ventricular function in all patients. <b>Conclusions:</b> Standardized totally endoscopic non-robotic mitral valve repair using the DCT approach was feasible and reproducible, achieving a 100% repair rate with favorable early outcomes. Given the single-center design and short follow-up, these should be interpreted as feasibility data.</p>","PeriodicalId":12669,"journal":{"name":"Global Cardiology Science & Practice","volume":"2026 4","pages":"e202630"},"PeriodicalIF":0.0000,"publicationDate":"2026-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13613133/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Global Cardiology Science & Practice","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21542/gcsp.2026.30","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: To evaluate early clinical and echocardiographic outcomes of totally endoscopic, non-robotic mitral valve repair for degenerative mitral regurgitation using a standardized DCT approach (double-port; camera and main working port in the same intercostal space; skin incision <3 cm), and to propose operational criteria for "totally endoscopic" mitral surgery. Methods: In this single-center observational study, 84 consecutive patients with severe degenerative mitral regurgitation meeting 2021 ESC/EACTS surgical criteria underwent totally endoscopic non-robotic repair with three-dimensional visualization between July 2023 and January 2026. The technique used a primary skin incision ≤3 cm with no rib spreading in all cases. Clinical and echocardiographic outcomes within 30 days were assessed. Results: Repair was successful in all 84 patients (100%), without conversion to sternotomy or replacement. All underwent ring annuloplasty; neochordal implantation was performed in 69 (82.1%). Mean incision length was 2.9 ± 0.3 cm. Mean cardiopulmonary bypass and cross-clamp times were 163.3 ± 50.5 and 112.1 ± 37.5 minutes, respectively. There was no 30-day mortality. Major complications each occurred in 1 patient (1.2%): re-exploration for bleeding, intracranial hemorrhage, and femoral artery occlusion. Median intensive care unit and hospital stays were 2 (IQR 2-3) and 10 (IQR 9-14) days. Echocardiography showed no residual regurgitation ≥ moderate and preserved ventricular function in all patients. Conclusions: Standardized totally endoscopic non-robotic mitral valve repair using the DCT approach was feasible and reproducible, achieving a 100% repair rate with favorable early outcomes. Given the single-center design and short follow-up, these should be interpreted as feasibility data.